Allele Registry

Canonical Allele Identifier: PA658816664

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000636164

RCV001775935

RCV002335884

RCV002343241

RCV003451522

RCV003454162

ClinVar Variation:

530347

1745212

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Gln169His	CA400484345 NM_032043.3:c.507G>T CA400484346 NM_032043.3:c.507G>C